- $106,390.00 - 159,250.00 / Year *
- Whippany, NJ 07981
* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.
Title: SAS Programmer in Whippany, NJ.Approx Contract Duration: Target 1 year.Description: The Contract SAS Programmer will work as part of a team of Data Management Programmers supporting all Data Management programming activities during the set-up, conduct and close-out of Phase I - IV clinical trials running across various therapeutic areas. Specific tasks performed include developing SAS programs (macros) to map all data collected by either our electronic data capture system (RAVE) or data captured by other central systems. For example, lab data, ECG data, PK data, Biomarker data. Data are transformed into one central Operational Acquisition Database (OAD) to meet the data structure standards for the specific drug project. Once this OAD database is built, additional programs are developed and run to check for consistency of data collected and also to check specific safety aspects. For example, reconciliation of Serious Adverse Events, medical review reports/listings/patient profiles. To prepare for the statistical analysis and also to verify quality of data collected compared to the protocol inclusion and exclusion criteria, additional reports are programmed to determine protocol deviations and validity of patients for analysis. Finally, after all data collection, mapping, edit checks, reporting is performed, the clinical database randomization is unblinded and Clean Database milestone is declared. Additionally the Contract SAS Programmer will be required to support quarterly Medicare reporting requirements via a SAS based reporting tool.Required Skills:1) 5 to 7 years of SAS programming experience within the Pharmaceutical industry/CRO supporting clinical trials. For example, working within the Data Management or Biostatistics functions.2) Oracle PL/SQL or Oracle LSH experience is a plus.3) Excellent knowledge of data management processes supporting Phase I-IV clinical trials.4) Extensive knowledge of CDISC SDTM data structures.5) Prior knowledge and experience of mapping of clinical trial data from legacy standards into conformant and compliant CDISC SDTM domains.6) Extensive knowledge and experience of performing validation. Knowledge of OpenCDISC checker or similar tools is a plus.7) Ability to lead projects.8) Self-motivated and a high commitment to quality and attention to detail.9) Ability to work on multiple projects at one time.10) Excellent verbal and written communication skills.11) Ability to work independently as well as part of a team environment.Min Salary: $0.00Max Salary: $0.00City: WhippanyState: NJ
Associated topics: data center, data engineer, data integration, data management, data scientist, database, erp, mongo database administrator, sql, sybase